A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17558687



Internal ID21883042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66904225..66904455hg38UCSC Ensembl
chr7:66369212..66369442hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38231
hg19231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6002677
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17558687
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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